Canonical Allele Identifier: CA934487488
Gene: SLC22A18 HGNC NCBI

Linked Data

dbSNP Id: rs1850002369

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2915776del , CM000673.2:g.2915776del GRCh38
NC_000011.9:g.2937006del , CM000673.1:g.2937006del GRCh37
NC_000011.8:g.2893582del NCBI36
NG_011512.1:g.21056del

Transcript Alleles

HGVS Amino-acid change
ENST00000649076.2:c.537-846del MANE Select ENSP00000497561.1:n.537-846del
ENST00000312221.9:c.537-846del ENSP00000311139.5:n.537-846del
ENST00000347936.6:c.537-846del ENSP00000307859.2:n.537-846del
ENST00000380574.5:c.537-846del ENSP00000369948.1:n.537-846del
ENST00000449793.6:c.243-846del ENSP00000392072.2:n.243-846del
ENST00000492567.2:n.507-433del
NM_001315501.1:c.792-846del NP_001302430.1:n.792-846del
NM_001315502.1:c.243-846del NP_001302431.1:n.243-846del
NM_002555.5:c.537-846del NP_002546.3:n.537-846del
NM_183233.2:c.537-846del NP_899056.2:n.537-846del
XM_005252953.3:c.107+520del XP_005253010.1:n.107+520del
XM_006718243.2:c.537-846del XP_006718306.1:n.537-846del
XM_011520140.1:c.735-846del XP_011518442.1:n.735-846del
XM_011520141.1:c.537-846del XP_011518443.1:n.537-846del
XM_011520142.1:c.537-846del XP_011518444.1:n.537-846del
XM_011520143.1:c.-424del XP_011518445.1:n.-424del
XM_011520141.2:c.792-846del XP_011518443.2:n.792-846del
XM_011520142.2:c.792-846del XP_011518444.2:n.792-846del
NM_001315502.2:c.243-846del NP_001302431.1:n.243-846del
NM_002555.6:c.537-846del MANE Select NP_002546.3:n.537-846del
NM_183233.3:c.537-846del NP_899056.2:n.537-846del
NM_001315501.2:c.792-846del NP_001302430.1:n.792-846del